DRI T-Uptake Calibrators

2.1 Classification of the substance or mixture

Regulation (EC) Mixture not yet fully tested. 1272/2008 [GHS] Directive 67/548/EEC or Mixture not yet fully tested. 1999/45/EC

CLP CLASSIFICATION

None required None required

Signal word

Warning SECTION 2 - HAZARDS IDENTIFICATION …continued Caution US Hazard overview Mixture not yet fully tested. This product contains human source material and should be treated/handled as a potential biohazard. Note This product/mixture does not meet criteria for classification according to Directive 1999/45/EC and Regulation EC No 1272/2008 (EU CLP). Nevertheless, it should be regarded as hazardous as it is potentially biohazardous and the pharmacological, toxicological, and ecological properties of this mixture have not been fully characterized. The CLP/GHS classifications are based on Regulation (EC) 1272/2008 and on the revised OSHA hazard communication standard. The EU symbol/indicator of danger, R Phrases and Safety Advice are based on Directive 1999/45/EC.

Hazard statements

CLP/GHS precautionary None required EU symbol/indication of None required danger Risk (R) Phrase(s) None required

Precautionary statements

None required

2.3 Other hazards

The potential health hazards associated with exposure/handling of this mixture are unknown; no data specific for the mixture were identified. The following data describe the hazards of individual ingredients, where applicable. This product/mixture contains human source material (human serum) and should be treated/handled as a potential biohazard. All such human source material has been derived from donors tested individually and shown by FDA approved methods to be free from antibodies to Human Immune Deficiency Virus and Hepatitis B and C. As no test method can offer complete assurance that these or other infectious agents are not present, this product should be handled using standard biosafety precautions.